Product Details

SNP ID

rs621999

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:78567912 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TATGCATTTGTGTACAACTGTCGTT[C/G]CATGTGGGTGGCTGAAAGTACTGTC

Phenotype

MIM: 118505

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

CHRNA5 PubMed Links

Additional Information

For this assay, SNP(s) [rs116297933] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

CHRNA5

Gene Name

cholinergic receptor nicotinic alpha 5 subunit

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000745.3		Intron			NP_000736.2
NM_001307945.1		Intron			NP_001294874.1
XM_005254142.3		Intron			XP_005254199.1
XM_017021881.1		Intron			XP_016877370.1

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